RFC2 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)

N° du produit ABIN2730775

Détail du produit

Antigène: RFC2 (Replication Factor C (Activator 1) 2, 40kDa (RFC2))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 2

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette RFC2 protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human RFC2 / RFC40 (transcript variant 2) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Détail du antigène

Antigène: RFC2 (Replication Factor C (Activator 1) 2, 40kDa (RFC2))

Autre désignation: Rfc2,rfc40 (RFC2 Produits)

Synonymes: 2610008M13Rik Protein, 40kDa Protein, AI326953 Protein, Recc2 Protein, RFC40 Protein, replication factor C subunit 2 Protein, replication factor C (activator 1) 2 Protein, LOC100231971 Protein, RFC2 Protein, Rfc2 Protein

Sujet: This gene encodes a member of the activator 1 small subunits family. The elongation of primed DNA templates by DNA polymerase delta and epsilon requires the action of the accessory proteins, proliferating cell nuclear antigen (PCNA) and replication factor C (RFC). Replication factor C, also called activator 1, is a protein complex consisting of five distinct subunits. This gene encodes the 40 kD subunit, which has been shown to be responsible for binding ATP and may help promote cell survival. Disruption of this gene is associated with Williams syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been described. A pseudogene of this gene has been defined on chromosome 2.

Poids moléculaire: 35.1 kDa

NCBI Accession: NP_002905

Pathways: Telomere Maintenance, Réparation de l'ADN, DNA Replication, Synthesis of DNA